Q: CO3(aq) NiCl3(aq) -->
A: Equation
Q: H*, H20
A: The reaction mechanism is as follows,
Q: d. 1. PhCO2Me NaOEt ELOH aq H* OEt 2. aq H*
A:
Q: (C) (A) (B) O₂N CO₂Me HNO 3 H₂SO4 SO 3 H₂SO4 Br 2 FeBr 3
A:
Q: H PhH₂CH₂C PhH₂CH₂C H 14 .... CH3 4 CH3 mcpba mcpba ? ? HT/H₂O H™/H₂O ? ?
A: Organic reactions are those in which organic reactant react to form organic products.
Q: k = Mh1
A: The unit of rate constant k = M h-1
Q: ( please explain both in detail)
A: Point group of a molecule is the indicative of symmetry operations present in the molecule.
Q: (a) (b) (c) (d) CH3 Br + H₂ + + CH3 RhCI(PPH3)3 Ru(=CHPH)Cl₂(PCY3)3 Br Pd(PPH3)2Cl2 B(OH)2 Pd(OAc)2
A:
Q: Br2 (1.0 equiv.), HOAC NaOAc H2O2 Br (aq., 30 wt-%, 5.5 equiv.) HO HO NaOH (1.5 equiv.), 20°C OMe…
A:
Q: Question attached
A: In the presence of strong acids, such as sulfuric acid and heat, alcohol dehydrates to an alkene.…
Q: (a) CEN-Ph CH2 NPh
A: Since you have posted multiple independent questions in the same request, we will solve the first…
Q: Draw all stereoisomers formed in each reaction.
A: All stereoisomers of given reaction can be drawn as
Q: elp?
A:
Q: What is the electrc H,C=CH,? The oloctron
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Q: पेह कर नाहटेकनांगवम वकढे Choze C००७९८ े ०fकठे न CH2I2 043
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Q: QUESTION 19 Briefly explain why there are + and - charges in the amino acid structures in the table…
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Q: A ) mePBA 2) Hcl/ THF Ch ater) B He and pd/C -> EtoH )ko BUABUOH 2) Btz then Fa 2/ NaoH/ HaO Br
A: A. Epoxidation olefin followed by epoxide opening with chloride ion. B. Hydrogenation of alkenes. C.…
Q: So (J/molK) So Organic Substance AHC AG ΔΗρ AGº Substance (kJ/mol) (kJ/mol) (kJ/mol) (kJ/mol)…
A: I had filled all the values is table Using the formula ∆G= ∆H-T∆S
Q: 16) K+ C2 KCI - - 17) Al + HCI → H2 + AICla - 18) N2+ F2 NF3 - - - 19) SO2 + LizSe> SSE2 + - Li20 -…
A: Balancing a chemical reactions includes making the number of atoms equal on each side of reaction
Q: d) e) f) CI NHCOPh
A:
Q: 4. CH3COOH(aq + C2H5OH CH3COOC2Hslag) + H2OM 5. AgCle) = Ag* (aa) + Ct (aq
A: The solution is given below -
Q: 20,²-(aq) + C,H;OH(aq) → CO29) + Cr³+
A: Cr2O72-(aq.)+ C2H5OH(aq.) ----> CO2(g) + Cr3+(aq.) Step-1: Split into half reaction and balanced…
Q: O a. -0.25
A: We know that Linkage disequilibrium measures the degree to which alleles at two loci are asociated.…
Q: G4 prepa ofoqMHcl in le D.wAtomic wt H=1ee:35
A: Molarity is defined as the number of moles of solutes present in per litre of solvent.
Q: a) CH2CH3 der. HBr ? Он b) `CH2OH PCC / CH2CI2 ? CH2OH c) 1) КMnOд / Н20 I NaOH / 25 °C `OH ? 2)…
A: a) Alcohol reacts with hydrogen bromide to form alkyl bromide.
Q: HCI(g) a. b. CH3F CH3OH с. H20 H2S
A: “Since you have posted a question with multiple sub-parts, we will solve the first three sub-parts…
Q: nich of the following co oduct? O 136-137 °C O 50 °C D 120 °C O 98-104 °C 116-117 °C
A: According to the question, a student synthesize an impure product of a compound with a melting point…
Q: 14СО, осcиr Occui
A:
Q: (aq) + CO2(g) + H2O(I).
A: Concentration(M) of HCl = 0.08586 M Volume(V) = 169 mL = 0.169 L Moles = M × V = 0.08586 × 0.169 =…
Q: Me NABH, i) MEOH i) CH3NH2 ii) ii) LIAIH4 iii) H20 HO. Br i) NaCN iv) HD D ii) H3O i) Base E v) OEt…
A:
Q: -5 Wihat PH ofa2.5NLO M NOOH Sudion? NoOH is a Strung lanse is the.
A:
Q: OH PDC HO. HO. но CH2CI2 HO, HO D
A: Given reaction,
Q: configuvation to fllowing Assign R oy S stauituus COOH b. •CH3 NH2
A: R and S nomenclature: it is used to assign the molecule using CIP rules. The CIP rules are as…
Q: •6rulfato lizand bedintimguinnod n How cen Itu ionie, nunodeutali and bidontali(cholaleci amd baid…
A: This Question is upon Inorganic IR Spectroscopy.
Q: A certain protein was found to contain 0.122%0.122% cobalt by mass. Determine the minimum molecular…
A: Mass percent can be expressed by the equation,
Q: Draw the organic products in each of the following reactions.
A: “Since you have asked multiple subparts, we will solve the first three for you. If you want any…
Q: H 138 NH₂ 121 H 140 i) (MeO)2SO2. ii) HCHO, HCI, DMF 189, 67% HN dioxane/H₂O, 60-80 °C 62-86%…
A: The first step of the synthesis is the condensation reaction between phenylhydrazine (138) and…
Q: Gणर नेह लाएhamiशरल पलकी Cvबी vowwd.and formatchatges. १) (৬) NaoH,H,0
A:
Q: C10H16B12 C C10H160 1. В1з, THF C10H180 F 2. Н2О2, НО E Br2 CH3CO0OH Br2 а-pinene C10H16 1. OsO4…
A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts…
Q: OH Oe Cadditiunal OH graup
A:
Q: маог MIInor В. O,N. NaBH4 B1 B2 B.
A: NaBH4 is a reducing agent which reduce aldehyde and ketones to respective alcohols.
Q: BEI Ho Exp
A: Mole is defined for the quantity of substance.
Q: Calculate AG°rxn
A:
Q: H. a. TiCl4, CH2CI2 -78 ° to 0 °C Cl.. b. H2O workup Me CHO Me
A: The mechanism of the reactions are given as
Q: acid FÓRMULA pKe1 pK.2 pK23 pK«4 Он HO-C-CH2-C–CH2–Ĉ–OH 2.94 4.14 5.82 16.0 0=C-OH
A: HA <===> H+ + A-
Q: CH3CO2H(aq) + NaOH(aq) → CH3CO (a - Nataq) + H201) (ад)
A:
Q: 1) 03, -78 °C H. ? 2) CH3SCH3
A: ->Ozonolysis of alkene produces carbony compound. In cinnamaldehyde there is present alkene which…
Q: OTBS PCC F) DCM, 25 °C 1) Hg(OAc)2. THF/H20 2) NABH4. Na OH TIPSOTI, pyridine H) DCM, 25 °C
A:
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- The two pentene isomers react with mCPBA, followed by an aqueous workup with NaOH/H2Ó. Draw the key reaction intermediates and the product(s); use arrow pushing to explain the stereochemical outcomes of the reactions Intermediate Final Products MCPBA CO2OH mCPBA NaOH/H2O CI Intermediate Final Products MCPBA NaOH/H2O 6.When treated with NaOH, the bromide below gives an alkene by the E2 mechanism, by elimination of the H atom indicated by the arrow: (a) Draw the Newman projection from which elimination takes place. (b) Draw the mechanism. (c) Draw the product with the proper stereochemistry. (d) Assign the proper stereochemical descriptor to the product. (e) Give the rate equationFor the following reaction, decide whether a solution of the products would be optically active or not and why. You will need to know the product of this reaction in order to solve this problem. To preview the image click here Br CH3 Na: CEN: acetone O Not optically active, achiral product is formed O Not optically active, racemic mixture is formed O Not optically active, a meso compound is formed O Optically active, a single enantiomer is formed
- For eaach image, predict the MAJOR product(s). Show stereochemistry where applicable and draw out ALL stereoisomers formed (as major products) in each reaction. State the mechanism(s) by which the major product(s) are formed (SN1, SN2, E1, and/or E2). Reagents are NOT present in excess.Draw the mechanism, including stereochemistry, of the following reaction, predicting the products formed. What is the relationship of the products that are formed?Consider the following reaction. CH3CH₂CH=CHCOH HCI CH3CH₂CH CHCOH c₁ CH3CH₂CH- H O CHCOH H CI this product is not observed Account for the fact that this reaction yields only a single product by drawing the carbocation intermediate leading to the observed product.
- When treated with NaOH, the bromide below gives an alkene by the E2 mechanism, by eliminationof the circled atoms: (a) Draw the Newman projection from which elimination takes place. (b) Draw the mechanism. (c) Draw the product with the proper stereochemistry. (d) Assign the proper stereochemical descriptor to the product. (Z, E? Trans,CiS?) (e)What would happen to the stereochemistry of the product if the enantiomer of the starting material were used inthe reaction?Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each of the following reactions (a-b): ? 1) RCO-H 2) [H₂SOJ Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. CH₂ Edit Drawing AIn the presence of light or heat, diazomethane (CH,N2) creates a carbene, which then adds to an alkene to make a cyclopropane. In the boxes below. draw the mechanism arrows for the reaction. H INEN: INE N:
- For each reaction, draw the complete mechanism and the major organic product(s), paying attention to stereochemistry. (a) (b) OH LOH (еxcess) ? ? CH,Cl2 CH2CI2Predict the major products of the following reaction. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products.Consider the elimination reaction shown below: Me- H2SO4 Ме— он Me alkene-containing product(s) heat, – H2O i) By providing a curly arrow mechanism, identify the two distinct alkene-containing products. ii) Identify the major product and explain why it is the major product.